| Literature DB >> 29477074 |
Rita Turnaturi1, Agostino Marrazzo2, Carmela Parenti3, Lorella Pasquinucci2.
Abstract
Benzomorphan, derived by morphine skeleton simplification, has been the subject of exploration in medicinal chemistry for the development of new drugs and pharmacological tools to explore opioid pharmacology in vitro and in vivo. Building upon these evidences, the design and synthesis of benzomorphan-based compounds, appropriately modified at the basic nitrogen and/or the phenolic hydroxyl (8-OH) group, represent a valid and versatile strategy to obtain analgesics. In this review, to improve the body of information in this field, we report structure activity-relationships (SARs) of benzomorphan-based compounds analysing data literature of last 25 years. Collectively, SARs data highlighted that the benzomorphan nucleus represents a template in the achievement of a specific functional profile, by modifying N-substituent or 8-OH group.Entities:
Keywords: Analgesia; Delta opioid receptor; Kappa opioid receptor; Mu opioid receptor; Pain; Structure activity relationship
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Year: 2018 PMID: 29477074 DOI: 10.1016/j.ejmech.2018.02.046
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514